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Volumn 523, Issue 2, 1996, Pages 167-178

Macrocyclic diphosphine ligands in asymmetric carbon-carbon bond-forming reactions

Author keywords

Asymmetric allylic alkylation; Chiral diphosphines; Macrocyclic ligands; Nickel; Palladium; X ray structural analyses

Indexed keywords


EID: 0030592426     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-328X(96)06251-1     Document Type: Article
Times cited : (46)

References (53)
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    • 5k
    • (d) [5k];
  • 38
    • 0011691452 scopus 로고    scopus 로고
    • Highest asymmetric inductions reported: (E)-pent-3-ene-2-yl acetate, 97% e.e. [5i]; 3-acetoxy-cyclohexene, 96% e.e. [5j]
    • [13] Highest asymmetric inductions reported: (E)-pent-3-ene-2-yl acetate, 97% e.e. [5i]; 3-acetoxy-cyclohexene, 96% e.e. [5j].
  • 41
    • 0011561790 scopus 로고    scopus 로고
    • Molecular modelling experiments were performed on a Silicon Graphics Workstation using the program SYBYL (Trypos) version 6.2; details will be published elsewhere
    • [15] Molecular modelling experiments were performed on a Silicon Graphics Workstation using the program SYBYL (Trypos) version 6.2; details will be published elsewhere.
  • 46
    • 0011561791 scopus 로고    scopus 로고
    • 10b
    • (b) [10b].
  • 47
  • 50
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    • 2
    • 2.
  • 51
    • 0004150157 scopus 로고
    • Siemens Crystallographic Research Systems
    • [24] (a) G.M. Sheldrick, SHELXTL-PC, Release 4.1, Siemens Crystallographic Research Systems, 1990;
    • (1990) SHELXTL-PC, Release 4.1
    • Sheldrick, G.M.1
  • 53
    • 0011567740 scopus 로고    scopus 로고
    • Supplementary data (bond length, bond angles, torsional angles and structure factors) have been deposited at the Cambridge Crystallographic Data Centre
    • [25] Supplementary data (bond length, bond angles, torsional angles and structure factors) have been deposited at the Cambridge Crystallographic Data Centre.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.